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首页> 外文期刊>Journal of Virological Methods >Analytical performance of newly developed multiplex human papillomavirus genotyping assay using Luminex xMAP (TM) technology (Mebgen((TM)) HPV Kit)
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Analytical performance of newly developed multiplex human papillomavirus genotyping assay using Luminex xMAP (TM) technology (Mebgen((TM)) HPV Kit)

机译:使用Luminex xMAP(TM)技术(Mebgen(TM)HPV试剂盒)的新开发的多重人乳头瘤病毒基因分型分析的分析性能

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摘要

Regional differences in human papillomavirus (HPV) genotypes and the presence of mixed HPV infections may affect adversely the efficacy of the HPV vaccine. Therefore, a simple and high-throughput HPV genotyping system is required. Recently, a novel HPV genotyping kit (the MebgenTm HPV kit) was developed. This kit uses multiplex PCR and Luminex xMAPTm technology to detect 13 types of high-risk HPVs and an internal control in a 96-well format. In the present study, the analytical performance of the kit was examined using HPV plasmid DNA. All 13 types of HPVs were detected with a minimum detection sensitivity of 250 copies/test, and highly specific signals were observed. HPV 16 plasmid was detected in samples containing mixtures with other HPV-type plasmids in ratios ranging from 1:1 to 1:1000. No cross reactivity was observed with DNA from 27 types of other infectious microbes. A clinical evaluation was carried out using cervical samples from 356 patients with persistent abnormal smears diagnosed at mass public health screenings for cervical cancer. The samples were preserved in TacasTm medium until analysis. HPV was detected in 162 (45.5%) samples including 110 (67.9%) with single infections and 52 (32.1%) with multiple infections. The type distribution of the 13 high-risk HPVs was as follows: 28.4% HPV 16, 11.7% HPV 18, 6.8% HPV 31,3.1% HPV 33,3.7% HPV 35,9.3% HPV 39, 1.9% HPV 45, 8.6% HPV 51, 37.0% HPV 52, 9.3% HPV 56, 16.7% HPV 58, 3.7% HPV 59, and 1.9% HPV 68. To evaluate sample stability over time, changes in the detection of HPV DNA derived from HeLa and SiHa cells were measured in 3 types of liquid-based cytology media. HPV DNA was detected in Tacas and ThinprepTm samples after storage at 4 C or 30 C for 4 weeks and within 1 week of collection in SurepathTM samples. These results suggest that this newly developed HPV genotyping kit is suitable for use in both clinical applications and large-scale epidemiological studies
机译:人乳头瘤病毒(HPV)基因型的区域差异和混合HPV感染的存在可能会对HPV疫苗的功效产生不利影响。因此,需要一种简单且高通量的HPV基因分型系统。最近,开发了一种新型的HPV基因分型试剂盒(MebgenTm HPV试剂盒)。该试剂盒使用多重PCR和Luminex xMAPTm技术以96孔格式检测13种类型的高风险HPV和内部对照。在本研究中,使用HPV质粒DNA检查了试剂盒的分析性能。以最低250拷贝/测试的检测灵敏度检测了所有13种HPV,并观察到了高度特异性的信号。在样品中检出的HPV 16质粒与其他HPV型质粒的混合物比例为1:1至1:1000。没有观察到来自27种其他感染性微生物的DNA的交叉反应性。使用从356例持续性异常涂片患者的宫颈样本中进行了临床评估,这些患者在大规模公共卫生筛查中被诊断为宫颈癌。将样品保存在TacasTm培养基中直至分析。在162(45.5%)个样本中检测到HPV,其中110个(67.9%)为单发感染,52(32.1%)为多发感染。 13种高危HPV的类型分布如下:28.4%HPV 16,11.7%HPV 18,6.8%HPV 31,3.1%HPV 33,3.7%HPV 35,9.3%HPV 39,1.9%HPV 45,8.6 HPV 51%,37.0%HPV 52、9.3%HPV 56、16.7%HPV 58、3.7%HPV 59和1.9%HPV68。为评估随时间变化的样品稳定性,请检测源自HeLa和SiHa细胞的HPV DNA检测的变化在3种基于液体的细胞学培养基中进行了测定。在Tacas和ThinprepTm样品中分别在4 C或30 C下储存4周后以及在SurepathTM样品中收集后1周内检测到HPV DNA。这些结果表明,这种新开发的HPV基因分型试剂盒适合在临床应用和大规模流行病学研究中使用

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